tert-Butyl (4-chlorocyclohexyl)carbamate CAS 35426-68-7

Purity 97%+In StockPharmaceutical Standards
CAS No.35426-68-7
Molecular FormulaC11H20ClNO2
Molecular Weight233.74 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl (4-chlorocyclohexyl)carbamate CAS 35426-68-7 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 233.74 g/mol gives tert-Butyl (4-chlorocyclohexyl)carbamate distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies tert-Butyl (4-chlorocyclohexyl)carbamate (CAS 35426-68-7), a certified reference material (molecular formula C11H20ClNO2, MW 233.74 g/mol) for analytical method development and quality control.

tert-Butyl (4-chlorocyclohexyl)carbamate (C11H20ClNO2) contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), tert-Butyl (4-chlorocyclohexyl)carbamate meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC11H20ClNO2
Molecular Weight233.74 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)2.0
CAS Registry Year (est.)1967
Halogen ContentCl-containing
Nitrogen Atoms1

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